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Results: 3โ€“4 Weeks Sample: Peripheral Whole Blood

Test Price

2,800 AED

โœ… Home Collection Available

๐Ÿ“‹ Results in 3โ€“4 Weeks

PRKAG2 Gene Cardiomyopathy, Familial Hypertrophic Type 6 Genetic Test in UAE | 2800 AED

Executive Summary & Core Metrics

  • Accuracy Guarantee: 99.9% diagnostic sensitivity via ISO 9001:2015 certified processing (INT/EGQ/2509DA/3139).
  • Premium Logistics: Hospital-grade cold-chain home collection & VIP mobile phlebotomy available daily 8 AMโ€“11 PM.
  • Clinical Guidance: Telephonic post-test result interpretation with a specialist genetics consultant.
  • Insurance: Direct billing verification via WhatsApp at +971 54 548 8731.
ISO 9001:2015 Certified DHA Compliant

Test Overview & Methodology

The PRKAG2 gene test uses next-generation sequencing (NGS) to detect pathogenic variants linked to familial hypertrophic cardiomyopathy type 6, a rare glycogen-storage disorder associated with arrhythmias, heart failure, and sudden cardiac death.

Feature Our Test (NGS-Based) Closest Alternative (Sanger Sequencing)
Methodology Next Generation Sequencing (NGS) โ€“ full coding region & splice sites Sanger sequencing of selected exons
Diagnostic Sensitivity 99.9% ~99%
Turnaround Time 3โ€“4 Weeks 6โ€“8 Weeks

Physician Insight & Safety Protocols

โ€œGenetic testing for PRKAG2 mutations provides critical insight into your risk profile, but it must be interpreted alongside a full cardiac evaluation, including ECG and imaging. A positive result does not guarantee disease expression; conversely, a negative result does not exclude all hereditary causes. Always discuss findings with a consultant medical geneticist before making lifestyle or treatment changes.โ€

โ€” Lina Osama Zaki Quteineh, Consultant Medical Genetics (DHA Registration ID: 9294403)

Medication Advisory

Do not discontinue any prescribed medication without consulting your doctor. Abrupt cessation may precipitate arrhythmias or heart failure decompensation.

Exclusion Criteria & Emergency Red Flags

  • Exclusion: Individuals unable to provide informed consent; minors without legal guardian consent.
  • Exclusion: Active febrile illness that may compromise sample integrity; defer blood draw until recovery.
  • Emergency Red Flags โ€“ seek immediate medical attention: new-onset severe chest pain, syncope, palpitations with dizziness, severe shortness of breath, or signs of stroke.

Patient FAQ & Clinical Guidance

1. What does the PRKAG2 gene test diagnose?

This test detects mutations in the PRKAG2 gene that cause familial hypertrophic cardiomyopathy type 6, a genetic heart muscle disorder marked by glycogen accumulation.

2. Is genetic counseling required before testing?

UAE guidelines recommend pre-test genetic counseling to discuss implications, obtain informed consent, and draw a detailed family pedigree to guide clinical interpretation.

3. How long does it take to get results?

Results are typically available within 3 to 4 weeks from sample receipt at our ISO-certified laboratory, ensuring thorough analysis and quality control.

4. What sample type is required?

A standard peripheral whole blood sample (5 mL in EDTA tube) is needed. Our VIP mobile phlebotomy service can collect this at your home in a temperature-controlled cold chain.

UAE Regulatory & Data Privacy Adherence

Regulatory Compliance: This test operates in full compliance with Federal Decreeโ€‘Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Clinical safety and patient consent follow Federal Decreeโ€‘Law No. 4 of 2016 on Medical Liability. All sample handling and laboratory processing are ISO 9001:2015 certified.

Clinical & Logistical Metadata

Test Name PRKAG2 Gene Cardiomyopathy, Familial Hypertrophic Type 6 Genetic Test
Price (AED) 2,800 AED
Turnaround Time 3โ€“4 Weeks
Sample Type / Matrix Peripheral Whole Blood โ€“ VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM)
Methodology Used Next Generation Sequencing (NGS) โ€“ full coding region & splice site analysis
ICD-10-CM Code I42.2
LOINC Code 55233-1
DHA Facility License & Laboratory Address DHA License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | Lab: DNA Labs UAE

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โœ… DHA Certified โœ… ISO 15189 โœ… HIPAA Compliant

Available in Arabic, English, Hindi & Urdu

Preparation Required

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Medically Reviewed by Dr. Lina Osama Zaki Quteineh

All content reviewed by qualified professionals for accuracy.

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All reports reviewed by DHA-Certified physicians